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Clefting disorders

Gene: RAI1

Red List (low evidence)

RAI1 (retinoic acid induced 1)
EnsemblGeneIds (GRCh38): ENSG00000108557
EnsemblGeneIds (GRCh37): ENSG00000108557
OMIM: 607642, Gene2Phenotype
RAI1 is in 8 panels

0 reviews

Details

Mode of Inheritance
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Red
Phenotypes
  • SMS
  • SMITH-MAGENIS SYNDROME
OMIM
607642
Clinvar variants
Variants in RAI1
Penetrance
None
Panels with this gene

History Filter Activity

16 Sep 2020, Gel status: 1

Created, Added New Source, Set mode of inheritance, Set Phenotypes

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: RAI1 was added gene: RAI1 was added to Clefting_GEL. Sources: Expert Review Red Mode of inheritance for gene: RAI1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Phenotypes for gene: RAI1 were set to SMS; SMITH-MAGENIS SYNDROME